21520-92-3 Usage
Chemical compound
2-Amino-5-(m-tolyl)oxymethyl-1,3,4-oxadiazole
Family
Oxadiazole
Structure
Consists of a five-membered ring containing two nitrogen atoms and an oxygen atom
Usage
Synthesis of pharmaceuticals and agrochemicals
Biological activities
Promising antimicrobial, anti-inflammatory, and anticancer properties
Potential medicinal applications
Treatment of neurological disorders
Pharmacological enhancement
Presence of the m-tolyl group
Overall assessment
Shows potential for various medicinal and agricultural applications
Check Digit Verification of cas no
The CAS Registry Mumber 21520-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,2 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21520-92:
(7*2)+(6*1)+(5*5)+(4*2)+(3*0)+(2*9)+(1*2)=73
73 % 10 = 3
So 21520-92-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3O2/c1-7-3-2-4-8(5-7)14-6-9-12-13-10(11)15-9/h2-5H,6H2,1H3,(H2,11,13)
21520-92-3Relevant articles and documents
Synthesis and Biological Activity of 3-Pentadecylaryloxyacetic Acids, Their Hydrazides and Cyclic Derivatives: Oxadiazoles and Pyrroles
Ramalingam, T.,Sattur, P. B.
, p. 1204 - 1207 (2007/10/02)
Several 3-pentadecylaryloxyacetic acids (III), their hydrazides (IV), 2-amino-5-(3'-pentadecylaryloxymethyl)-1,3,4-oxadiazoles (V) and 1-(3'-pentadecylaryloxyacetamido)-2,5-dimethylpyrroles (VI) have been synthesised and evaluated for their biological activity.Some of the compounds exhibit strong antiinflammatory action in experimental animals.Presence of a long alkyl chain (C13H31) renders the compounds to be less toxic.
On knowledge of 2-amino-1,3,4-oxidazole. 25. 2-amino-5-aryloxy(thio)alkyl-1,3,4-oxdiazole
Gehlen,Uteg
, p. 911 - 922 (2007/10/06)
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